Optical Coherence Tomography in Inflammatory and Neoplastic Lesions Deforming the Choroidal Profile

The choroid is the main part of the uvea, the vascular layer of the eye that lies between the retina and the sclera. The high vascular component of the choroid makes this structure susceptible to inflammation in multisystemic diseases, as well as the most common site of metastasis in the eye. Therefore, the choroid is involved in many pathological conditions, from uveitis to intraocular tumors. Differentiating between inflammatory and neoplastic lesions deforming the choroidal profile can sometimes be challenging. In addition, scleral disorders can also deform the choroidal profile. Choroidal imaging includes ophthalmic ultrasonography, indocyanine green angiography, and optical coherence tomography (OCT). Recent advances in choroidal imaging techniques, such as enhanced depth imaging optical coherence tomography (EDI-OCT) and swept-source optical coherence tomography (SS-OCT), have facilitated an in-depth analysis of the choroid. The purpose of this review article is to report on and highlight the most common OCT findings to help in the differential diagnosis between inflammatory and neoplastic lesions deforming the choroidal profile.


Introduction
The choroid is the largest and most posterior portion of the uvea, the vascular layer of the eye that lies between the retina and the sclera that nourishes the retinal pigment epithelium (RPE) and the outer retina. The high vascular component of the choroid makes this structure susceptible to inflammation in multisystemic diseases, as well as the most common site of metastasis in the eye [1].
The inaccessibility of the choroidal structure to direct clinical examination makes clinicians rely on imaging techniques for its evaluation. Traditional choroidal imaging modalities include indocyanine green angiography (ICGA) and ocular ultrasonography (US) [2]. More recently, the non-invasive optical coherence tomography (OCT) has been introduced. OCT uses the principle of low coherence interferometry to obtain in-depth information from various retinal structures to create cross-sectional images [2].
Conventional spectral-domain OCT (SD-OCT) has some limitations, especially in the evaluation of deeper structures such as the choroid. Enhanced depth imaging OCT (EDI-OCT) uses a scanning position closer to the eye to create an inverted SD-OCT image with the advantage of better depth sensitivity.

Chronic Recurrent Uveitic Phase of VKH Disease
Initial-onset acute VKH disease is characterized by early posterior uveitis, whi not properly controlled, can be followed by the chronic recurrent phase of the disease anterior segment inflammation [4]. Using ICGA, Bacsal et al. and Takemoto et al. sho concomitant subclinical choroidal inflammation in patients with anterior segment r rence [11,12]. Choroidal thickness increases during the anterior uveitis attack, then creases when the inflammation has resolved after treatment [12]. Instead, choroidal cularity index (CVI) decreases during the anterior uveitis attack, returning to baseline ues after treatment [13].
Sakata et al. reported a unique finding in VKH patients in the non-acute uveitic s "choroidal bulging", which seems to be related to active posterior segment inflamma It is characterized by a localized thickening of the choroid, which assumes a conve pearance with consequent bulging of the RPE/Bruch's membrane reflective comple Fluorescein angiography (FA) features indicate secondary retinal involvement as a consequence of severe choroiditis, including subretinal fluid pooling due to ERD and optic disc hyperfluorescence ( Figure 1B,E). ICGA reveals signs of choroiditis characterized by the presence of hypofluorescent dark dots and vasculitis of choroidal vessels (fuzziness of the vessels) ( Figure 1C,F) [5]. B-scan US of the eye displays ERD with associated diffuse low-to-medium reflective thickening of the choroid posteriorly [6].
In acute VKH disease associated uveitis, OCT shows ERD with subretinal fluid compartments separated by the typical septa ( Figure 1G). Tsuboi et al. have described choroidal folds, which may be the result of a thickened choroid compressing Bruch's membrane and RPE causing undulations of the RPE ( Figure 1H). Choroidal folds were quantified using the RPE undulation index [7].
OCT can also be helpful in the early recognition of the predominantly optic disc swelling variant, which carries a worse prognosis [8]. In the acute phase of VKH disease, EDI-OCT reveals a markedly diffuse thickening of the choroid. Choroidal thickness may serve as a marker for the degree of choroidal inflammation, which gradually decreases with treatment ( Figure 1I,J) [9]. SS-OCT provides better resolution images of the choroid than EDI-OCT does, resulting in more measurable images. When both SS-OCT and EDI-OCT images are readable, the measurements are comparable [10].

Chronic Recurrent Uveitic Phase of VKH Disease
Initial-onset acute VKH disease is characterized by early posterior uveitis, which, if not properly controlled, can be followed by the chronic recurrent phase of the disease with anterior segment inflammation [4]. Using ICGA, Bacsal et al. and Takemoto et al. showed concomitant subclinical choroidal inflammation in patients with anterior segment recurrence [11,12]. Choroidal thickness increases during the anterior uveitis attack, then decreases when the inflammation has resolved after treatment [12]. Instead, choroidal vascularity index (CVI) decreases during the anterior uveitis attack, returning to baseline values after treatment [13].
Sakata et al. reported a unique finding in VKH patients in the non-acute uveitic stage, "choroidal bulging", which seems to be related to active posterior segment inflammation. It is characterized by a localized thickening of the choroid, which assumes a convex appearance with consequent bulging of the RPE/Bruch's membrane reflective complex anterior ( Figure 2) [14].
During the convalescent stage in patients with long-standing VKH disease, the choroid thickness turned out to be progressively thinner on EDI-OCT than that of normal individuals [15].

Isolated Tubercular and Sarcoid Choroid Granulomas
Tuberculosis (TB) and sarcoidosis are chronic multisystem granulomatous diseases that share similar pulmonary and extrapulmonary manifestations, including choroidal involvement in uveitis [16,17]. The prevalence of TB uveitis (TBU) is estimated to be between 9% and 11% in endemic countries and between 1% and 6% in non-endemic countries [18]. Choroiditis is its most frequent manifestation [19]. Choroidal involvement in TBU can involve the choriocapillaris in serpiginous-like and ampiginous choroiditis or the stromal choroid in cases of choroidal granuloma, recently termed "tuberculoma" by the Collaborative Ocular Tuberculosis Study (COTS) group [20].
Ocular sarcoidosis shows a wide range of clinical manifestations, including uveitis, and can precede systemic involvement in 12-30% of cases [21]. Isolated choroidal granuloma, which can be the first manifestation of the disease, is a relatively rare lesion that occurs in approximately 5% of cases of sarcoid uveitis [22].
On eye fundus examination, tuberculoma appears as a solitary, large (up to 14 mm) yellowish round-shaped subretinal lesion, commonly seen at the posterior pole and occasionally in periphery ( Figure 3A) [20]. On FA, active tuberculomas show an early hypofluorescence with late hyperfluorescence, while inactive healed tuberculomas show transmission hyperfluorescence ( Figure 3B,C) [25]. On ICGA, tuberculoma appears as an oval or round hypofluorescent lesion, both in the early and late phases of the exam (full thickness choroidal granuloma) ( Figure 3E,F) [25]. Fundus examination, FA, and ICGA of isolated sarcoid choroidal granuloma are identical to choroidal tuberculoma [26].

Isolated Tubercular and Sarcoid Choroid Granulomas
Tuberculosis (TB) and sarcoidosis are chronic multisystem granulomatous diseases that share similar pulmonary and extrapulmonary manifestations, including choroidal involvement in uveitis [16,17]. The prevalence of TB uveitis (TBU) is estimated to be between 9% and 11% in endemic countries and between 1% and 6% in non-endemic countries [18]. Choroiditis is its most frequent manifestation [19]. Choroidal involvement in TBU can involve the choriocapillaris in serpiginous-like and ampiginous choroiditis or the stromal choroid in cases of choroidal granuloma, recently termed "tuberculoma" by the Collaborative Ocular Tuberculosis Study (COTS) group [20].
Ocular sarcoidosis shows a wide range of clinical manifestations, including uveitis, and can precede systemic involvement in 12-30% of cases [21]. Isolated choroidal granuloma, which can be the first manifestation of the disease, is a relatively rare lesion that occurs in approximately 5% of cases of sarcoid uveitis [22].
On eye fundus examination, tuberculoma appears as a solitary, large (up to 14 mm) yellowish round-shaped subretinal lesion, commonly seen at the posterior pole and occasionally in periphery ( Figure 3A) [20]. On FA, active tuberculomas show an early hypofluorescence with late hyperfluorescence, while inactive healed tuberculomas show transmission hyperfluorescence ( Figure 3B,C) [25]. On ICGA, tuberculoma appears as an oval or round hypofluorescent lesion, both in the early and late phases of the exam (full thickness choroidal granuloma) ( Figure 3E,F) [25]. Fundus examination, FA, and ICGA of isolated sarcoid choroidal granuloma are identical to choroidal tuberculoma [26]. On EDI-OCT and SS-OCT images, choroidal tuberculoma appears as a hyporeflective lesion involving the choroidal stroma that exhibits increased signal transmission ( Figure 3G,H) [27]. OCT is also helpful in detecting outer retinal changes above the tuberculoma. Salman et al. were the first to describe the "contact sign" as localized hyperreflective material, suggestive of inflammatory infiltrate, in a contact area between the choriocapillaris/RPE complex and the overlying neurosensory retina above the choroidal granuloma associated with surrounding subretinal fluid [28]. Subsequently, Agarwal et al. described the possible fluid accumulation within the photoreceptor layer with a split involving the myoid zone of the photoreceptors [25], termed "bacillary layer detachment" by Mehta et al. in their description of toxoplasma chorioretinitis and pachychoroid disease [29].
Isolated sarcoid choroidal granuloma on EDI-OCT images shares similarities with tuberculoma. It appears as a hyporeflective thickening of the choroid, responsible for a dome-shape appearance of the overlaying retina and RPE. The adjacent choroid has normal thickness and reflectivity. The outer retinal layers overlying the choroidal lesion can be hyperreflective, suggestive of inflammatory infiltrate [30].
Non-invasive follow-up during treatment can be performed with EDI-OCT or SS-OCT to evaluate the improvement of the granuloma (hyporeflective choroidal lesion, subretinal fluid, outer retinal layer changes) or the development of complications (choroidal neovascular membrane or subretinal abscess in cases of TB) [31].
dome-shape appearance of the overlaying retina and RPE. The adjacent choroid has normal thickness and reflectivity. The outer retinal layers overlying the choroidal lesion can be hyperreflective, suggestive of inflammatory infiltrate [30].
Non-invasive follow-up during treatment can be performed with EDI-OCT or SS-OCT to evaluate the improvement of the granuloma (hyporeflective choroidal lesion, subretinal fluid, outer retinal layer changes) or the development of complications (choroidal neovascular membrane or subretinal abscess in cases of TB) [31].

Scleral Inflammatory Lesions
In posterior scleritis, inflammation can spread to the adjacent choroid, causing the following different manifestations of choroidal involvement: (1) increased choroidal thickness, (2) choroidal vasculitis, (3) presentation as a choroidal or subretinal mass in nodular

Nodular Posterior Scleritis
Nodular posterior scleritis is a rare unilateral inflammatory condition affecting only a part of the sclera posterior to the equator, in contrast with diffuse posterior scleritis [33]. Disease onset is generally in the fifth decade of life, with a marked predominance in females. Only a few cases of nodular posterior scleritis have been reported in the literature [34]. The scleral nodule can mimic a choroidal mass, and the rapid recognition of the disease avoids invasive diagnostic surgical procedures, such as chorioretinal biopsy, to exclude neoplastic disorders [35][36][37][38]. A hallmark symptom of nodular posterior scleritis is pain with headache, generally absent in intraocular neoplastic (amelanotic melanoma, choroidal metastasis, choroidal hemangioma, choroidal osteoma) or other inflammatory (choroidal granuloma) conditions [39]. Likewise, the presence of conjunctival injection, chemosis, and limited extraocular motility guides the clinician toward the diagnosis of scleritis instead of neoplastic conditions [40].
On fundus examination, the scleral nodule appears as an isolated amelanotic subretinal mass in the absence of lipofuscin or drusen, with possible associated ERD or reti-Diagnostics 2023, 13, 1991 6 of 15 nal/choroidal folds ( Figure 4A) [41]. Clinical signs/symptoms (pain) and multimodal imaging (MMI) can help in the differential diagnosis of scleral nodules with intraocular tumors [33].
late phases due to choroidal inflammation and leakage from the large choroidal vessels [33].
B-scan US, a key exam for the diagnosis and follow-up of the scleral lesion, may show sessile unilobed lesion with high reflectivity and, only in 36% of cases, edema in sub-Tenon's space ('T' sign) ( Figure 4C). Computerized tomography (CT) scan and magnetic resonance imaging (MRI) of the orbit with contrast show scleral thickening and are important as complementary exams to rule out choroidal masses [34].
EDI-OCT and SS-OCT can show an elevated profile of the retina due to the subretinal lesion with a normal choroid tissue beneath it ( Figure 4D) and occasionally focal or multifocal ERD, retinal/choroidal folds, or macular edema ( Figure 4E) ( Table 1).  The combination of FA and ICGA is important to rule out dual circulation, which is a classical finding of choroidal melanoma. The scleral nodule may present with multiple areas of pinpoint leakage and diffuse pooling in the area of the ERD. Occasionally, it is possible to observe optic disc swelling and macular edema. ICGA can show an early hypofluorescence at the location of the ERD and areas of pinpoint hyperfluorescence during late phases due to choroidal inflammation and leakage from the large choroidal vessels [33].
B-scan US, a key exam for the diagnosis and follow-up of the scleral lesion, may show sessile unilobed lesion with high reflectivity and, only in 36% of cases, edema in sub-Tenon's space ('T' sign) ( Figure 4C). Computerized tomography (CT) scan and magnetic resonance imaging (MRI) of the orbit with contrast show scleral thickening and are important as complementary exams to rule out choroidal masses [34].
EDI-OCT and SS-OCT can show an elevated profile of the retina due to the subretinal lesion with a normal choroid tissue beneath it ( Figure 4D) and occasionally focal or multifocal ERD, retinal/choroidal folds, or macular edema ( Figure 4E) ( Table 1).

Choroidal Melanoma
Choroidal melanoma is a life-threatening malignancy generally diagnosed on clinical examination by means of fundus examination and ultrasonography. It usually presents as a pigmented (85%), sessile, or dome-shaped lesion characterized by overlying orange pigment and complicated by ERD. US is useful for determining size, thickness, and basal dimension and to exclude extraocular extension. On B-scan US, the dome-shaped profile is the most common, but mushroom/collar stud-shaped is the most classic shape; an irregular shape is uncommon. The tumor typically presents medium-to-low homogeneous internal reflectivity on A-scan US. On MRI, it appears hyperintense on T1-weighted images and hypointense on T2-weighted images.
FA pattern in choroidal melanoma is influenced by tumor size and pigmentation, associated ERD, and hemorrhages. In the early phase, it typically shows irregular hyperfluorescence in cases of RPE/outer retinal atrophy, with variable leakage in late phases. Hypofluorescent spots may be seen due to clumps of orange pigment or pigment mottling. Early frames of ICGA demonstrate hypofluorescence of the lesion and sometimes the intrinsic choroidal vasculature, while in the late phase, different patterns can be observed. Nevertheless, neither FA nor ICGA is considered diagnostic.
EDI-OCT of choroidal melanoma generally shows smooth-surface topography with optical shadowing and compression of the overlying choriocapillaris ( Figure 5). In a review of EDI-OCT features of small choroidal melanomas, Shields et al. reported that subretinal fluid, lipofuscin deposition, and retinal irregularities, such as shaggy photoreceptors, were common findings. Shaggy photoreceptors overlying choroidal melanoma could represent edematous photoreceptors or macrophages with lipofuscin on the posterior surface of the detached retina and were more frequently found in choroidal melanoma (49%) than in choroidal nevus (0%). Small choroidal melanoma tumor thickness was overestimated by 55% on US compared with EDI-OCT [42].

Choroidal Metastasis
Choroidal metastases are the most frequent form of intraocular malignancy; they generally appear as a small-to-medium size creamy white or pale-yellow mass with poorly defined margins, mean thickness of 3 mm, located posteriorly or at the equator, and are often associated with overlying subretinal fluid.
Choroidal metastases are characterized by a flatter or slightly dome-shaped mass on B-scan US and by medium-to-high nonhomogeneous internal reflectivity on A-scan US. These metastases are mostly multilobular with an irregular surface and may be multifocal and/or bilateral. view of EDI-OCT features of small choroidal melanomas, Shields et al. reported that subretinal fluid, lipofuscin deposition, and retinal irregularities, such as shaggy photoreceptors, were common findings. Shaggy photoreceptors overlying choroidal melanoma could represent edematous photoreceptors or macrophages with lipofuscin on the posterior surface of the detached retina and were more frequently found in choroidal melanoma (49%) than in choroidal nevus (0%). Small choroidal melanoma tumor thickness was overestimated by 55% on US compared with EDI-OCT [42].

Choroidal Metastasis
Choroidal metastases are the most frequent form of intraocular malignancy; they generally appear as a small-to-medium size creamy white or pale-yellow mass with poorly defined margins, mean thickness of 3 mm, located posteriorly or at the equator, and are often associated with overlying subretinal fluid.
Choroidal metastases are characterized by a flatter or slightly dome-shaped mass on B-scan US and by medium-to-high nonhomogeneous internal reflectivity on A-scan US. These metastases are mostly multilobular with an irregular surface and may be multifocal and/or bilateral.
FA and ICGA are useful in documenting these lesions. FA typically shows hypofluorescence with mottled hyperfluorescence in correspondence with RPE defects in early phases and irregular hyperfluorescence in the late phases, with possible leakage and pooling in the subretinal space. On ICGA, choroidal metastases appear as well-defined areas of hypofluorescence, with no intrinsic vasculature during all angiogram phases. Minor staining of the lesion may be noticed in the late frames of the angiogram [43,44]. FA and ICGA are useful in documenting these lesions. FA typically shows hypofluorescence with mottled hyperfluorescence in correspondence with RPE defects in early phases and irregular hyperfluorescence in the late phases, with possible leakage and pooling in the subretinal space. On ICGA, choroidal metastases appear as well-defined areas of hypofluorescence, with no intrinsic vasculature during all angiogram phases. Minor staining of the lesion may be noticed in the late frames of the angiogram [43,44].
The diagnosis is mainly clinical, but EDI-OCT studies have significantly improved the diagnostic ability to detect small lesions. US overestimates the thickness of small metastatic tumors by a mean of 59% when compared with EDI-OCT. In addition, EDI-OCT is more sensitive than US in the evaluation of recent-onset lesions and response after treatment [45].

Choroidal Hemangioma
Choroidal hemangioma is a benign vascular tumor of the choroid, classified as circumscribed or diffuse depending on its distribution and clinical appearance. Choroidal hemangioma may occur sporadically or in combination with Sturge-Weber disease. The circumscribed choroidal hemangioma appears clinically as a round or oval red-orange mass with indistinct margins, classically located posterior to the equator in the macular or paramacular region of the eye. Typically, the diagnosis occurs when the lesion is complicated ses, barely seen with indirect ophthalmoscopy [46]. The rippled irregular surface appearance, often labeled as a "lumpy bumpy" profile, can be a feature of choroidal metastasis on EDI-OCT. Other lesions with rippled surface include choroidal lymphoma, uveal effusion, hypotony maculopathy, and some forms of uveal inflammatory disease [47]. In choroidal metastasis, EDI-OCT showed a minimally "lumpy bumpy" surface topography with overlying subretinal fluid and shaggy photoreceptors [48]. Low internal optical reflectivity (71%), plateau shape tumor elevation with flat wavy RPE apical surface (75%), overlying choriocapillaris thinning (100%), and partial choroidal shadowing underneath the tumor (71%) were the other common EDI-OCT features in metastatic choroidal tumors ( Figure 6) [45].

Choroidal Hemangioma
Choroidal hemangioma is a benign vascular tumor of the choroid, classified as circumscribed or diffuse depending on its distribution and clinical appearance. Choroidal hemangioma may occur sporadically or in combination with Sturge-Weber disease. The circumscribed choroidal hemangioma appears clinically as a round or oval red-orange mass with indistinct margins, classically located posterior to the equator in the macular or paramacular region of the eye. Typically, the diagnosis occurs when the lesion is complicated by intra-or subretinal exudation, resembling central serous chorioretinopathy. Choroidal hemangioma can also simulate an amelanotic choroidal melanoma or metastasis. FA does not add significant information as it shows varying degrees of hyperfluorescence in all phases. There is early lacy mild hyperfluorescence in the pre-arterial or early arterial phase and diffuse intense hyperfluorescence in the late phase [49]. The ICGA pattern is pathognomonic, showing a rapid lobular filling, with early intense hyperfluorescence in the first minute and a "washout" effect with reduction of the hyperfluorescence in the late phases of the ICGA (30 min) (Figure 7) [49].
On MRI, it appears hyperintense to vitreous on T1 and hyper-isointense on T2 with contrast enhancement [49,50]. On B-scan US, choroidal hemangioma appears as a domeshaped acoustically solid mass similar to the surrounding normal choroid. On A-scan US, it has high internal reflectivity [51]. Compared to US, tumor thickness measurement by EDI-OCT was 51% less than on US [52].
Rojanaporn et al. reported that on EDI-OCT, choroidal hemangioma shows a smooth, gently sloping anterior contour (100%) with gradual expansion of medium and large size choroidal vessels without compression of the choriocapillaris (100%). The lumen of the choroidal vessels in the choriocapillaris, Haller's layer, and Sattler's layer were expanded rather than compressed, as is seen with nevus, melanoma, and metastasis. Other OCT features included partial optical shadowing underneath the hemangioma (90%), subretinal fluid (70%), lipofuscin deposition (10%), intact Bruch's membrane, and structural abnormalities of outer and inner retinal layers related to chronic subretinal fluid (Figure 7) [52]. gently sloping anterior contour (100%) with gradual expansion of medium and large size choroidal vessels without compression of the choriocapillaris (100%). The lumen of the choroidal vessels in the choriocapillaris, Haller's layer, and Sattler's layer were expanded rather than compressed, as is seen with nevus, melanoma, and metastasis. Other OCT features included partial optical shadowing underneath the hemangioma (90%), subretinal fluid (70%), lipofuscin deposition (10%), intact Bruch's membrane, and structural abnormalities of outer and inner retinal layers related to chronic subretinal fluid (Figure 7) [52].

Choroidal Lymphoma
Choroidal lymphoma is a rare ocular malignancy, most commonly of B cell origin, that usually appears as amelanotic infiltration of the posterior uvea. It is classified as primary choroidal lymphoma (69%), typically a low grade lymphoma (extranodal marginal zone B-cell lymphoma is the predominant form), or secondary choroidal lymphoma (31%) in the presence of systemic, often high grade lymphoma [47].
Funduscopic findings include multifocal creamy-yellow patches at the level of choroid, ERD, and less frequently, choroidal folds. A detailed clinical examination can be suggestive of choroidal lymphoma, but a definitive diagnosis can only be obtained with biopsy and cytologic evaluation.
The main differential diagnosis includes inflammatory diseases such as birdshot choroidopathy, acute multifocal placoid pigment epitheliopathy, and intraocular tumors, including choroidal metastases, melanoma, and hemangioma. Multifocal yellow-white subretinal infiltrates are also commonly seen in vitreoretinal lymphoma; however, in this condition, the infiltrates are typically located between the RPE and the Bruch's membrane rather than in the choroid [53].
FA can reveal multiple pinpoint leakages, followed by pooling of the dye as well as optic disc staining. Choroidal infiltration on ICGA is characterized by multifocal sub-millimeter hypofluorescent round areas (300-500 microns diameter) that may resemble a granulomatous uveitis [54,55]. The typical B-scan US appearance is an acoustically hollow thickening of the choroid that, in some cases, can show extrascleral extension [53]. US and MRI show a relatively smooth surface of this malignancy.
EDI-OCT has a sufficiently high resolution (down to the 4 mm level) to demonstrate how the tumor surface varies depending on tumor thickness [56]. Shields et al. described the surface topography of choroidal lymphoma, comparing its features to the ocean surface as calm, rippled, or undulating (seasick). In thin lymphoma infiltration (mean: 1.7 mm), the choroidal surface appeared calm, in medium infiltration (mean: 2.8 mm) it appeared rippled, and in thick infiltration (mean: 4.1 mm) it was undulating or "seasick" [47]. The irregular undulating appearance is most characteristic of choroidal lymphoma but can occasionally be found in choroidal metastasis, choroidal osteoma, and sclerochoroidal calcification, although to a lesser degree [47]. Moreover, in choroidal lymphoma, the choriocapillaris is compressed inward on EDI-OCT images, while medium and large choroidal vessels are generally not detectable.

Conclusions
The differential diagnosis between inflammatory and neoplastic lesions deforming the choroidal profile can sometimes be challenging. Distinguishing between these conditions is essential for the correct management of the patient and is driven by an accurate clinical examination in association with the support of MMI. The more recently introduced EDI-OCT and SS-OCT imaging modalities provide a deeper penetration and a better resolution of the choroid, resulting in improved characterization of subretinal lesions deforming the choroidal profile (Table 3). Table 3. OCT imaging findings of inflammatory and neoplastic lesions. Informed Consent Statement: Informed consent was obtained from all subjects to publish any accompanying images at the Ocular Immunology Unit, Azienda Unità Sanitaria Locale (AUSL)-IRCCS di Reggio Emilia, Italy.
Data Availability Statement: Not applicable.